Office for Clinical Research

弗吉尼亚大学(UVA)癌症中心临床研究室的总体目标 将提供一个中央临床研究基础设施，以： ？促进研究性临床研究的启动和管理 协助癌症中心首席研究人员和临床医生进行患者筛选和登记 关于临床研究的研究 ？结合《议定书》监测临床试验所有监管方面的遵守情况 审查委员会、IRB、州和联邦指南 ？为参与临床研究的所有癌症中心工作人员提供培训和教育计划 研究 ？为内部和外部质量保证审计提供支持 ？向癌症中心医生传达临床研究研究的可用性，参考 医生和社区 ？推荐、开发、实施和维护最先进的信息系统，以支持 癌症临床研究的工作流程、数据共享、分析和报告要求 对Forte Research Systems，OnCore临床研究管理系统的用户进行培训

The overall objectives of the University of Virginia (UVA) Cancer Center's Office of Clinical Research (OCR) are to provide a central clinical research infrastructure to: ¿ Facilitate the activation and administration of research clinical studies ¿ Assist Cancer Center Principal Investigators and clinicians in the screening and enrolling of patients on clinical research studies ¿ Monitor compliance with all regulatory aspects of clinical trials in conjunction with the Protocol Review Committee, IRB, state, and federal guidelines ¿ Provide a training and education program for all Cancer Center staff involved in clinical research studies ¿ Provide support for internal and external quality assurance audits ¿ Communicate the availability of clinical research studies to Cancer Center physicians, referring physicians, and the community ¿ Recommend, develop, implement, and maintain state-of-the-art information systems to support the workflow, data sharing, analyses, and reporting requirements of cancer clinical research studies ¿ Train users on the Forte Research Systems, OnCore¿ clinical research management system